Soluble VCAM-1 alters lipid phosphatase activity in epicardial mesothelial cells: Implications for lipid signaling during epicardial formation

Manjari Ranganathan, Danijela Dokic, Sonia W. Sterrett, Kathryn L. Dwyer, Robert W. Dettman*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Epicardial formation involves the attachment of proepicardial (PE) cells to the heart and the superficial migration of mesothelial cells over the surface of the heart. Superficial migration has long been known to involve the interaction of integrins expressed by the epicardium and their ligands expressed by the myocardium; however, little is understood about signals that maintain the mesothelium as it migrates. One signaling pathway known to regulate junctional contacts in epithelia is the PI3K/Akt signaling pathway and this pathway can be modified by integrins. Here, we tested the hypothesis that the myocardially expressed, integrin ligand VCAM-1 modulates the activity of the PI3K/Akt signaling pathway by activating the lipid phosphatase activity of PTEN. We found that epicardial cells stimulated with a soluble form of VCAM-1 (sVCAM-1) reorganized PTEN from the cytoplasm to the membrane and nucleus and activated PTEN's lipid phosphatase activity. Chick embryonic epicardial mesothelial cells (EMCs) expressing a shRNA to PTEN increased invasion in collagen gels, but only after stimulation by TGFß3, indicating that loss of PTEN is not sufficient to induce invasion. Expression of an activated form of PTEN was capable of blocking degradation of junctional complexes by TGFß3. This suggested that PTEN plays a role in maintaining the mesothelial state of epicardium and not in EMT. We tested if altering PTEN activity could affect coronary vessel development and observed that embryonic chick hearts infected with a virus expressing activated human PTEN had fewer coronary vessels. Our data support a role for VCAM-1 in mediating critical steps in epicardial development through PTEN in epicardial cells.

Original languageEnglish (US)
Pages (from-to)159-185
Number of pages27
JournalJournal of Developmental Biology
Volume1
Issue number2
DOIs
StatePublished - Sep 1 2013

Keywords

  • CD106/VCAM-1
  • Epicardium
  • PIP
  • PTEN
  • Phosphatidylinositol phosphate

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

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